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The Japanese Journal of Human Genetics|March 1, 1997
Detection of the CTG repeat expansion in congenital myotonic dystrophyK Ohya, N Tachi, T Sato, et al.
The Tohoku Journal of Experimental Medicine|January 1, 1985
An application of fluorescein-conjugated monoclonal antibodies to the diagnosis of Chlamydia trachomatis infection in childrenK Numazaki, S Chiba, T Moroboshi, et al.
No to Hattatsu = Brain and Development|November 1, 1990
[Benign familial neonatal convulsion: clinical features of the propositus and comparison with the previously reported cases]S Wakai, N Tachi, Y Ishikawa, et al.
Pediatric Neurology|May 1, 1997
Haplotype analysis of congenital myotonic dystrophy patients from asymptomatic DM fatherN Tachi, K Ohya, H Yamagata, et al.
Neuropediatrics|November 1, 1985
A case of childhood multiple sclerosis with peripheral neuropathyN Tachi, Y Ishikawa, A Tsuzuki, et al.
Pediatric Neurology|February 22, 2001
Expression of peripheral myelin protein zero in sural nerve of patients with Charcot-Marie-Tooth disease 1BN Tachi, N Kozuka, K Ohya, et al.
Comparative Biochemistry and Physiology. Toxicology & Pharmacology : CBP|February 13, 2001
Antihypertensive effect of ACE inhibitory oligopeptides from chicken egg yolksH Yoshii, N Tachi, R Ohba, et al.
Acta Paediatrica Japonica : Overseas Edition|April 1, 1992
Severe neonatal nemaline myopathy--histological and histochemical studies of respiratory musclesN Tachi, S Wakai, Y Watanabe, et al.
Acta Paediatrica Japonica : Overseas Edition|February 1, 1997
Detection of the mutation in facioscapulohumeral muscular dystrophy patientsK Ohya, N Tachi, N Kozuka, et al.
No to Shinkei = Brain and Nerve|May 1, 1997
[Locations of crossover breakpoints within the CMT 1 A-REP repeat in patients with hereditary neuropathy with liability to pressure palsy--detection by recombinant chromosome-specific polymerase chain reaction]M Yamamoto, T Yasuda, T Mitsuma, et al.
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